Potassium peroxymonosulfate

Bromide ndIodide. The spectrophotometric determination of trace bromide concentration is based on the bromide catalysis of iodine oxidation to iodate by permanganate in acidic solution. Iodide can also be measured spectrophotometricaHy by selective oxidation to iodine by potassium peroxymonosulfate (KHSO ). The iodine reacts with colorless leucocrystal violet to produce the highly colored leucocrystal violet dye. Greater than 200 mg/L of chloride interferes with the color development. Trace concentrations of iodide are determined by its abiUty to cataly2e ceric ion reduction by arsenous acid. The reduction reaction is stopped at a specific time by the addition of ferrous ammonium sulfate. The ferrous ion is oxidi2ed to ferric ion, which then reacts with thiocyanate to produce a deep red complex. 

Potassium peroxymonosulfate, introduced in the late 1980s, is finding increasing use as an auxiUary oxidant for shock treatment and oxidation of chloramines. Sodium peroxydisulfate is also being sold for shock treatment, however, it is less reactive than peroxymonosulfate. Mixtures of sodium peroxydisulfate and calcium hypochlorite can be used for shock treatment (28). Disadvantages of peroxymonosulfate and peroxydisulfate are they do not provide a disinfectant residual and peroxymonosulfate oxidizes urea and chloramines to nitrate ion, which is a nutrient for algae. 

Oxidation of Chlorides. Hypochlorite can also be formed by the in situ oxidation of chloride ions by potassium peroxymonosulfate [25482-78-4] (36). Ketones like acetone cataly2e the reaction (37). The triple salt of potassium peroxymonosulfate is a stable powder that has been combiaed with chloride salts and sold as toilet bowl cleaners. Bromides can be used ia place of chlorides to form hypobromites, and such combiaations are used to disiafect spas and hot tubs. 

Lithium hypochlorite, halogenated hydantoias, potassium peroxymonosulfate, and hydrogen peroxide. 

Surface disinfectants Compounds containing phenolics, chlorhexidine (not effective against bacteria spores), quaternary ammonium salts (additional activity if bis-n-tributyltin oxide present), hypochlorites such as household bleach, alcohols such as 70-95% ethanol and isopropyl (not effective against bacteria spores), potassium peroxymonosulfate, hydrogen peroxide, iodine/iodophores, and triclosan. 

Tetrahydrobenzyl alcohol (( )3-cyclohexenene-l-methanol) and 30% aqueous hydrogen peroxide were purchased from Fluka, AG. 3-Cyclohexene-1-carboxylic acid and cis-4-cyclohexene-l,2-dicarboxylic acid were used as purchased from Lancaster Chemical Co. Methyl iodide, acetic anhydride, Oxone (potassium peroxymonosulfate), Aliquot 336 (methyl tri-n-octylammonium chloride), sodium tungstate dihydrate and N,N-dimethylaminopyridine (DMAP) were purchased from Aldrich Chemical Co. and used as received. 3,4-Epoxycyclohexylmethyl 3, 4 -epoxycyclohexane carboxylate (ERL 4221) and 4-vinylcyclohexene dioxide were used as purchased from the Union Carbide Corp. (4-n-Octyloxyphenyl)phenyliodonium hexafluoroantimonate used as a photoinitiator was prepared by a procedure described previously (4). 

Potassium peroxomonosulfate, 14 67 Potassium peroxydisulfate, 14 292 Potassium peroxymonosulfate, 26 189 Potassium persulfate, 7 856 Potassium phosphates, 18 834-835 20 637 manufacture of, 18 854 Potassium polymetaphosphate, 18 848 Potassium products, 20 5991 Potassium pyrophosphates, 18 843 Potassium residues, 20 603 Potassium salts, 20 609... 

Oxone (potassium peroxymonosulfate, 2 KHSO5KHSO4K2SO4) was purchased from Aldrich Chemical Company, Inc. 

Oxone is a registered trademark of DuPont with potassium peroxymonosulfate KHSOs (potassium monopersulfate) as oxidizing ingredient of a triple salt with the formula... 

All forms of iodine including the elemental iodine, hypoiodous acid (HOI), hypoiodite anion (OI ), free iodide anion (I-), and triiodide anion (I3 ) in water also may be measured by the Leuco crystal violet method. The sample is treated with potassium peroxymonosulfate to oxidize all iodide species in the sample. It then is treated with leukocrystal violet reagent for color development. Interference from free chlorine may be eliminated by addition of an ammonium salt. 

Potassium ozonide, 735 Potassium permanganate chemiluminescence, 643 hydrogen peroxide titration, 627 ozonide redox titration, 736 Potassium peroxymonosulfate, dioxirane preparation, 26, 1020-30, 1130 Potassium superoxide, commercial availability, 620... 

Sulfides in the electrophilic positions are often oxidized to sulfones to facilitate nucleophilic displacement reactions. The sulfoxide is initially formed, and can sometimes be isolated, but normally the oxidation is allowed to proceed fully to give the sulfone. Peroxyacids are commonly used as the oxidant, although other reagents such as oxone (potassium peroxymonosulfate) can also be employed <20030L1011, 2006ARK(vii)452>. 

Both isomeric forms of (+)- and (—)-(camphorylsulfonyl)oxaziridines are available by oxidation of the corresponding sulfonimines with buffered potassium peroxymonosulfate (oxone). Since oxidation can only take place from the endo-fa.ce of the C=N double bond due to steric blocking of the exo-face, a single oxaziridine isomer is obtained. The enantiomerically pure sulfonimines can be prepared in three steps in better than 80% yield from inexpensive (+)- and (—)-camphor-10-sulfonic acids. Alternatively they are commercially available200. 

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